A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059334



Internal ID18801865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:82277007..82411683hg38UCSC Ensembl
Innerchr17:80234883..80369559hg19UCSC Ensembl
Innerchr17:77828172..77962848hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38134677
hg19134677
hg18134677
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3567891, nssv3567892
Samples
Known GenesCD7, OGFOD3, SECTM1, TEX19, UTS2R
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059334
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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